The Gonorrhea Rapid Test Device(Swab)uses highly specific antigen-antibody reaction
and immune chromatography analysis techniques for the qualitative detection of whether
clinical specimens contain Gonorrhea trachomatis antigen, and the kit contains Gonorrhea
trachomatis antigen-specific antibodies,which are pre-fixed on the test area (T) on the membrane,and the corresponding antibodies on the quality control area (C). During the detection,the pyrolysis-off specimens on the cotton swab are titrated into the sampling
wells (S) of the kit, and the specimens make a specific antibody reaction with the
Gonorrhea trachomatis antigen of the pre-coated gold particles.Then, the mixture followed up with upward chromatography under capillary effect. If it is positive , gold-labeled Gonorrhea will first bind with Gonorrhea trachomatis antigen in the specimens in the
chromatography process, then the bonder will be combined by specific antibody of Gonorrhea trachomatis antigen, which is fixed on the membrane, and within the test
area (T) there will appear a red band. If it is negative, there will no red band within the test
area (T). Regardless of whether the Gonorrhea trachomatis antigen exists in clinical
samples, there will be a red band within the quality control area (C). The red bandwithin the quality control area (C) is to determine whether there is sufficient sample,
and whether the process of chromatography is in line with the normal standards, and at the
same time it is used as the internal control standards of the agent.